Run ID: SRR1141261
Sample name:
Date: 02-04-2023 21:00:16
Number of reads: 82560
Percentage reads mapped: 1.18
Strain: lineage4.9
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.97 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 1.0 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 1.0 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 1.0 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 1.0 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 1.0 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 1.0 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 1.0 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 1.0 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.93 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.91 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.89 |
rpoB | 763123 | p.Ile1106Thr | missense_variant | 1.0 |
rpoC | 764332 | c.963G>A | synonymous_variant | 0.67 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.67 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.67 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 1.0 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.67 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 1.0 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.67 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.67 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.67 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.67 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.79 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.94 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.86 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.88 |
rpoC | 764672 | p.Gln435Thr | missense_variant | 0.96 |
rpoC | 764686 | c.1317C>T | synonymous_variant | 0.82 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.93 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.95 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.92 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.92 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.86 |
rpoC | 764858 | p.Leu497Met | missense_variant | 0.75 |
rpoC | 764875 | c.1506C>G | synonymous_variant | 1.0 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 1.0 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 1.0 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
rpoC | 764912 | p.Met515Val | missense_variant | 1.0 |
rpoC | 764918 | p.Val517Ile | missense_variant | 1.0 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.93 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.92 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 0.92 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.92 |
rpoC | 764958 | p.Glu530Ala | missense_variant | 0.92 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.92 |
rpoC | 764995 | c.1626C>T | synonymous_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472709 | n.864T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475787 | n.2130C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.89 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.8 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2221939 | p.Arg409Gln | missense_variant | 1.0 |
thyA | 3073953 | c.519T>C | synonymous_variant | 1.0 |
thyA | 3073956 | c.516G>C | synonymous_variant | 1.0 |
thyA | 3073959 | c.513T>C | synonymous_variant | 1.0 |
thyA | 3073962 | p.Leu170Ile | missense_variant | 1.0 |
thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
thyA | 3073992 | c.478_480delAGCinsTCG | synonymous_variant | 1.0 |
thyA | 3073999 | p.Arg158Lys | missense_variant | 1.0 |
thyA | 3074004 | c.468T>C | synonymous_variant | 1.0 |
thyA | 3074010 | c.462C>G | synonymous_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4039691 | c.1014G>T | synonymous_variant | 0.67 |
clpC1 | 4039697 | c.1008C>T | synonymous_variant | 0.67 |
clpC1 | 4039700 | c.1005C>T | synonymous_variant | 0.67 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.5 |
clpC1 | 4039727 | c.978C>T | synonymous_variant | 0.5 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.5 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.5 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |